血浆射流与n -乙酰半胱氨酸联合作用对HepG2癌细胞凋亡和增殖的控制

Q1 Medicine
Zilan Xiong , Shasha Zhao
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引用次数: 0

摘要

众所周知,常压等离子体可诱导癌细胞凋亡。[1][2]然而,血浆与癌细胞之间的相互作用及其机制尚不完全清楚。[3]本文报道了He/O2等离子射流与n -乙酰半胱氨酸(NAC,自由基清除剂)联合治疗对人肝癌细胞(HepG2)凋亡和增殖的控制作用。发现血浆处理时间和NAC预处理可以控制HepG2细胞的命运。纯血浆处理可诱导HepG2细胞凋亡。然而,NAC预处理的15s血浆一方面与NAC浓度有一定的关系,可以促进HepG2细胞的增殖。另一方面,nac预处理可以通过长时间血浆处理(如>240s)明显降低细胞凋亡作用,而未观察到细胞增殖。NAC和15s等离子体处理加速了HepG2细胞G1期向S期的转变,导致细胞增殖,而长时间等离子体处理使细胞周期停留在G2/M期,导致细胞凋亡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Controlling of apoptosis and proliferation of HepG2 cancer cells by treatment of plasma jet and N-acetylcysteine combination

It is well known that atmospheric pressure plasma could induce apoptosis of cancer cells. [1][2] However, the interaction and mechanism between plasma and cancer cells has not been fully understood yet. [3] Here, we report the controlment of apoptosis and proliferation of human hepatocellular carcinoma cell (HepG2) by combined treatment of He/O2 plasma jet and N-acetylcysteine (NAC, free radical scavenger). It is found that the fate of HepG2 cells could be controlled by plasma treatment time together with NAC pretreatment. Pure plasma treatment could induce apoptosis of HepG2 cells. However, on one hand, 15s plasma with NAC pre-treatment could enhance proliferation of HepG2 cell as a function of NAC concentration. On the other hand, NAC-pretreatment could markedly compromise apoptosis effect by long time plasma treatment (e.g. >240s) without proliferation observed. The NAC and 15s plasma treatment accelerates the G1 to S phase transition of HepG2 cells causing proliferation while long time plasma treatment arrests the cell cycle at the G2/M phase inducing apoptosis.

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来源期刊
Clinical Plasma Medicine
Clinical Plasma Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
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